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Stable Au(I) catalysts for oxidant-free C-H Functionalization with Iodoarenes.
Mertens, R Tyler; Greif, Charles E; Coogle, James T; Berger, Gilles; Parkin, Sean; Watson, Mark D; Awuah, Samuel G.
Afiliación
  • Mertens RT; Department of Chemistry, University of Kentucky, Lexington, KY 40506 USA.
  • Greif CE; Department of Chemistry, University of Kentucky, Lexington, KY 40506 USA.
  • Coogle JT; Department of Chemistry, University of Kentucky, Lexington, KY 40506 USA.
  • Berger G; Department of Medicinal Chemistry, Université libre de Bruxelles.
  • Parkin S; Department of Chemistry, University of Kentucky, Lexington, KY 40506 USA.
  • Watson MD; Department of Chemistry, University of Kentucky, Lexington, KY 40506 USA.
  • Awuah SG; Department of Chemistry, University of Kentucky, Lexington, KY 40506 USA.
J Catal ; 408: 109-114, 2022 Apr.
Article en En | MEDLINE | ID: mdl-35368720
ABSTRACT
The development of oxidant-free gold-catalyzed cross coupling reactions involving aryl halides have been hamstrung by the lack of gold catalysts capable of performing oxidative addition at Au(I) centers. Herein, we report the development of novel tricoordinate Au(I) catalysts supported by N,N-bidentate ligands and ligated by phosphine or arsine ligands for C-H functionalization without external oxidants to form biaryls with no homocoupling. The unsymmetrical character of the Au(I) catalyst is critical to facilitating this necessary orthogonal transformation. This study unveils yet another potential of Au(I) catalysis in biaryl synthesis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Catal Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Catal Año: 2022 Tipo del documento: Article